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List of works by Allison Brashear

A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1.

scientific article published on 24 December 2015

ATP1A3 Mutation in Adult Rapid-Onset Ataxia

scientific article (publication date: 2016)

ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.

scientific article

ATP1A3 mutations: what is the phenotype?

scientific article published on 15 January 2014

ATP1A3-Related Neurologic Disorders

scientific article published on 22 February 2018

Alternating Hemiplegia of Childhood in a Person of Malay Ethnicity with Diffusion Tensor Imaging Abnormalities.

scientific article

Auditory-perceptual voice and speech evaluation in ATP1A3 positive patients

scientific article published on 05 October 2020

Author response

Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study

scientific article published on 10 September 2020

Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism

article

Cognitive impairment in rapid-onset dystonia-parkinsonism

scientific article published on 16 January 2014

Comparison of treatment of tardive dystonia and idiopathic cervical dystonia with botulinum toxin type A ⬇️

scientific article published on 01 January 1998

Distinct neurological disorders with ATP1A3 mutations

scientific article

Dystonia & tremor: A cross-sectional study of the dystonia coalition cohort

scientific article published on 12 October 2020

Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition

scientific article published on 16 August 2019

Genotype-structure-phenotype relationships diverge in paralogs , , and

Metrifonate treatment of AD: influence of APOE genotype

scientific article published in December 1999

Misfolding, altered membrane distributions, and the unfolded protein response contribute to pathogenicity differences in Na,K-ATPase ATP1A3 mutations

scientific article published on 03 November 2020

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

scientific article

New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism.

scientific article published on 24 April 2012

Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly

scientific article

PET imaging of the pre-synaptic dopamine uptake sites in rapid-onset dystonia-parkinsonism (RDP).

scientific article

Psychiatric disorders in rapid-onset dystonia-parkinsonism ⬇️

scientific article published on August 29, 2012

Rapid onset dystonia parkinsonism in a 14-year-old girl

scholarly article by D W Webb et al published January 1999 in European Journal of Paediatric Neurology

Rapid-Onset Dystonia-Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation.

scientific article published on 30 December 2014

Rapid-onset dystonia-parkinsonism

scientific article published on 01 December 1993

Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings

scientific article

Rapid-onset dystonia-parkinsonism in a second family.

scholarly article by A Brashear et al published 1997 in Neurology

Rapid-onset dystonia-parkinsonism: a fourth family consistent with linkage to chromosome 19q13.

scientific article

Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two families

scientific article published on 01 January 1998

Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13

scientific article (publication date: August 1999)

Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders

scientific article

Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing

scientific article published on 30 July 2019

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

scientific article

Variable phenotype of rapid-onset dystonia-parkinsonism

scholarly article by A Brashear et al published March 1996 in Movement Disorders

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